Recordkeeping Requirements for Producers, Registrants, and Applicants of Pesticides and Pesticide Devices under Section 8 of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) (Renewal)
ICR 201407-2070-001
OMB: 2070-0028
Federal Form Document
⚠️ Notice: This information collection may be outdated. More recent filings for OMB 2070-0028 can be found here:
Recordkeeping Requirements
for Producers, Registrants, and Applicants of Pesticides and
Pesticide Devices under Section 8 of the Federal Insecticide,
Fungicide, and Rodenticide Act (FIFRA) (Renewal)
Extension without change of a currently approved collection
FIFRA section 8 states that the
Administrator of the Environmental Protection Agency may prescribe
regulations requiring pesticide producers, registrants and
applicants for registration to maintain such records with respect
to their operations and the effective enforcement of this Act and
to make such records available for inspection and copying as
specified in the statute. The regulations at 40 CFR Part 169 (Books
and Records of Pesticide Production and Distribution) specify the
following records that producers must keep and the disposition of
those records. Producers must maintain records on production data
for pesticides, devices, or active ingredients (including
pesticides produced pursuant to an experimental use permit);
receipt by the producer of pesticides, devices, or active
ingredients used in producing pesticides; delivery, moving, or
holding of pesticides; inventory; domestic advertising for
restricted use pesticides; guarantees; exports; disposal; human
testing; and tolerance petitions. Additionally, section 8 gives the
Agency inspectional authority to monitor the validity of research
data (including raw data), developed in accordance with Good
Laboratory Practice Standards, and used to support pesticide
registration. These records generally consist of the material
produced during the course of ordinary business activity, and are
maintained in the location, manner, and duration as is generally
prudent for such records in the course of ordinary business
activity. Respondents are required to maintain records of receipt,
production, shipping, and inventory for two years. Records
regarding testing of registered pesticides must be maintained for
the life of the pesticide registration, as such data are necessary
to support the regulatory decision. Approximately 11,600
respondents are currently subject to this requirement, and it is
estimated that no additional respondents per year will become
subject to this requirement in the next three years. The cost of
this ICR to the respondents is estimated to be $1,762,040. The
estimate of number of respondents is based on the number of
pesticide producers who have responded to the latest mandatory
annual reporting response under FIFRA section 7, which defines the
entire universe of legal producers of pesticides for sale or
distribution in the United States. The estimated change is based on
extrapolation from trends in the number of reported producers over
the last three years. The estimated cost per producer has been
estimated to consist entirely of the cost of preparing records for
inspection, as the recordkeeping itself consists of activities that
are considered to be customary business practices.
PL:
Pub.L. 61 - 158 8 Name of Law: Federal Insecticide, Fungicide,
and Rodenticide Act
There is an increase of 5,694
hours in the total estimated respondent burden compared with the
ICR currently approved by OMB. This increase is due to the growth
in the number of respondents since the last ICR.
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.